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Completed

NCT Number: NCT05990335

Boost Study 21270 (Cognition)

This study is designed to to test the technical feasibility of encouraging interaction with a mobile smartphone software package (mHealth app) for training aspects of executive function and cognition.

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Key information

Conditions

Cognitive Function Abnormal Cognition Disorders Mental Disorders Neurocognitive Disorders

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Early Phase 1

Primary location

Kansas State DPS

Manhattan, Kansas, 66506, United States

About this study

The purpose of this human subjects study is to test the technical feasibility of interaction with a mobile smartphone software package (mHealth app) for training in aspects of executive function and cognition. The study participants are healthy subjects recruited online, with consent secured at the time of screening, and with enrollees assigned to High or Low groups on the basis of initial screening task scores. Subjects are requested to participate in directed interaction activities for up to 8 weeks, with measures primarily evaluating feasibility of MHealth app package task completion and secondarily evaluating the cognitive effect of activities.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 18 years and above
  • Fluent in English
  • Resides in the United States
  • Score on prescreen task is in 25% quartile
  • Familiar with smartphone device app installation and device usage
  • Possesses a compatible smartphone

Exclusion criteria

None

Treatment and study plan

mHealth application (custom)

Behavioral

Smartphone based application designed to engage user executive functions

Primary outcomes

  1. Task Completion Rate

    Time frame: At 8 weeks

    Percentage of participants completing minimum required weekly interactions

Secondary outcomes

  1. Change in Task Performance

    Time frame: At 8 weeks

    Change in Human Hypothetical Choice scale (higher scores indicate a better outcome, minimum value 0 to maximum value 1), calculated as value at 8 weeks minus value at 1 week

Sponsors and collaborators

Lead sponsor

NXTech

Industry

Collaborators

  • Kansas State University
  • National Institute on Drug Abuse (NIDA)
  • National Institutes of Health (NIH)

Registry information

Official study title

Mobile Software Application Intervention Including Cognitive Tasks

Important dates

Study start
2022
Primary completion
2023
Study completion
2023
First posted
Aug 14, 2023
Registry last updated
Dec 18, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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